Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs11594656 0.776 0.240 10 6080046 intergenic variant T/A snv 0.18 9
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs1980422 0.776 0.320 2 203745673 intergenic variant C/A;T snv 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8